GLP Study Director

Job content

GLP Study Director, Bradford

Grow a Better Tomorrow with Nufarm.

We know that growing is about more than just crops and cultivation. It’s about sunshine and rain, early mornings and hard work. It can be frustratingly unpredictable but also wonderfully uplifting. More than anything, it’s about people. Nufarm is the dependable partner behind thousands of agricultural success stories. Every day, growers around the world turn to our products and our people to help with the challenges of fighting disease, weeds and pests, and to increase crop yields.

How can you grow with Nufarm?

If you join our expanding site as a GLP Study Director, you will be responsible for ensuring GLP studies are conducted according to the Principles of Good Laboratory Practice and agreed protocols using appropriate validated analytical methodologies and prepare the final reports for submission to regulatory authorities.

What will you be doing?

Ensure that GLP studies are conducted to the required guidelines using appropriate validated analytical methodologies in a safe manner, adhering to the Study Director’s responsibilities detailed in Schedule 1 of the Good Laboratory Practice regulations.

Ensure that regulatory deadlines are met through communication with sponsors and organising personal workload efficiently.

Prepare analytical reports for submission to regularity authorities to facilitate timely registration of products worldwide.

Ensure that samples are prepared, stored and utilised correctly and that study data are recorded, interpreted and documented in an appropriate manner according to the principles of GLP.

Undertake method development and method validation activities in relation to the analysis of active substances and formulations including the determination of low level impurities.

Ensure the validation, maintenance and service of analytical equipment within the GLP laboratory has been conducted in accordance with the appropriate SOPs.

Supervise and/or train GLP analysts undertaking analysis intended for use in GLP studies.

Respond to comments and questions from sponsors and regulatory authorities as appropriate with respect to study reports produced.

Be the point of study control with sponsors and have overall responsibility for the scientific, technical and regulatory conduct of studies.

What do you bring?

To be our GLP Study Director you must have 2+ years of study director experience in GLP lab. Experience working in a regulatory environment, managing studies that are compliant with GLP.

You will be a graduate chemist significant knowledge and experience gained in an analytical laboratory, preferably in a GLP or similarly regulated environment. You will have experience in HPLC, GC, GC/MS analysis and experience in the writing and interpretation of technical reports and standards operating procedures.

The team is a close-knit team of professionals so communication and working well in a team are important. This role also has supervisory responsibilities of GLP Analysts so you will have leadership skills.

Salary and benefits

Working as a GLP Study Director means receiving a comprehensive benefits package alongside your salary. This includes pension, annual bonus, and health care scheme amongst others. In addition to this 28-day annual leave including bank holidays.

We are an equal opportunity employer, and we value diversity. All employment decisions are decided based on qualifications, merit and business needs. We are committed to building an inclusive environment for all Nufarm employees.

If you want to be a part of a thriving, supportive environment and are inspired by the prospect of being a part of something bigger, we’d love to hear from you.

We are an equal opportunity employer and we value diversity. All employment decisions are decided based on qualifications, merit and business needs. We are committed to building an inclusive environment for all Nufarm employees.